跳至主要内容
临床试验/CTRI/2025/08/093085
CTRI/2025/08/093085
尚未招募
不适用

Evaluation of Comparative Efficacy of Mulligan Mobilization, Maitland Mobilization, High Velocity Thrust, and Muscle Energy Technique on Disability, Pain and Displacement of Center of Gravity in Subjects with Sacroiliac Dysfunction - A Four Arm Parallel Trial

Datta Meghe Institute of Higher Education and Research1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年8月28日最近更新:

概览

阶段
不适用
状态
尚未招募
发起方
Datta Meghe Institute of Higher Education and Research
入组人数
120
试验地点
1
主要终点
1. VISUAL ANALOGUE SCALE (VAS)

概览

简要总结

Sacroiliac dysfunction is a condition in which the movement between the sacrum and iliac bones is affected, leading to pain and dysfunction. The problem is often masked by low back pain. Specific treatment approaches for sacroiliac dysfunction include mobilization, exercise prescription, and electrotherapeutic management. This is a four-arm parallel trial conducted to establish the rank order between four physiotherapy interventions given for sacroiliac dysfunction. Outcome measures to assess will be the pain rating scale, disability index, and Center of gravity. based on the outcomes. To determine the significance of the difference between the four groups, the student t" test will be employed. We will compare the parameters among the three groups using a paired "t" test. Repeated measures of ANOVA will be employed to determine the significance of changes between pre- and post-treatment. Rank order will be established post study.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 35.00 Year(s)(—)
性别
All

入选标准

  • Patients willing to sign informed consent
  • Patients diagnosed with sacroiliac dysfunction.
  • Both males and females between the age of
  • 35 years.
  • Patients on which Gaenselin’s and Gillet’s test is positive.
  • Patients with non-specific low back pain, and stiff back region for at least 3 months.

排除标准

  • Patients with a recent history of surgery on the back region.
  • Post-traumatic back pain and stiffness.
  • Patients with Lumbar radiculopathy
  • Patients with a previous history of fracture at the lower limb or back region.
  • Patients with pathology related to the spine.

结局指标

主要结局

1. VISUAL ANALOGUE SCALE (VAS)

时间窗: All outcomes will be assessed Pre-intervention | on 1st day, post | intervention on 21st day, and post | intervention on 60th day

2.Modified Oswestry Disability Index

时间窗: All outcomes will be assessed Pre-intervention | on 1st day, post | intervention on 21st day, and post | intervention on 60th day

3.Center of Gravity (COG)

时间窗: All outcomes will be assessed Pre-intervention | on 1st day, post | intervention on 21st day, and post | intervention on 60th day

次要结局

未报告次要终点

研究者

发起方
Datta Meghe Institute of Higher Education and Research
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Neha Chitale

Ravi Nair Physiotherapy College, Datta Meghe Institute of Higher Education and Research

研究点 (1)

Loading locations...

相似试验